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Institution

Universidade Federal de Minas Gerais

EducationBelo Horizonte, Minas Gerais, Brazil
About: Universidade Federal de Minas Gerais is a education organization based out in Belo Horizonte, Minas Gerais, Brazil. It is known for research contribution in the topics: Population & Context (language use). The organization has 41631 authors who have published 75688 publications receiving 1249905 citations.


Papers
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Journal ArticleDOI
TL;DR: Experimental results are presented that showpolygonal mobile robots controlled using visual feedback, transporting a convex polygonal object in an obstacle free environment toward a prescribed goal.
Abstract: In this paper we address the problem of transporting objects with multiple mobile robots using the concept of “object closure”. In contrast to other manipulation techniques that are typically derived from form or force closure constraints, object closure requires the less stringent condition that the object be trapped or caged by the robots. Our basic goal in this paper is to develop decentralized control policies for a group of robots to move toward a goal position while maintaining a condition of object closure. We present experimental results that show polygonal mobile robots controlled using visual feedback, transporting a convex polygonal object in an obstacle free environment toward a prescribed goal.

188 citations

Journal ArticleDOI
TL;DR: Creating and strengthening indigenous lands and other protected areas represents an effective, practical, and immediate REDD strategy that addresses both biodiversity and climate crises at once.
Abstract: Recent climate talks in Copenhagen reaffirmed the crucial role of reducing emissions from deforestation and degradation (REDD). Creating and strengthening indigenous lands and other protected areas represents an effective, practical, and immediate REDD strategy that addresses both biodiversity and climate crises at once.

188 citations

Journal ArticleDOI
TL;DR: Recent advances in the understanding of resolution of inflammation are reviewed, highlighting the pharmacological strategies that may interfere with the molecular pathways which control leukocyte survival and clearance and suggesting that pharmacological modulation of the resolution process may be useful for the treatment of chronic inflammatory diseases in humans.

187 citations

Journal ArticleDOI
TL;DR: The results indicate that T.cruzi parasites elicit an alternative inflammatory pathway independent of TLR2 that is partially dependent on MyD88 and necessary for mounting optimal inflammatory and RNI responses that control T. cruzi replication during the early stages of infection.
Abstract: Studies performed in vitro suggest that activation of Toll-like receptors (TLRs) by parasite-derived molecules may initiate inflammatory responses and host innate defense mechanisms against Trypanosoma cruzi. Here, we evaluated the impact of TLR2 and myeloid differentiation factor 88 (MyD88) deficiencies in host resistance to infection with T. cruzi. Our results show that macrophages derived from TLR2 (-/-) and MyD88(-/-) mice are less responsive to GPI-mucin derived from T. cruzi trypomastigotes and parasites. In contrast, the same cells from TLR2(-/-) still produce TNF-alpha, IL-12, and reactive nitrogen intermediates (RNI) upon exposure to live T. cruzi trypomastigotes. Consistently, we show that TLR2(-/-) mice mount a robust proinflammatory cytokine response as well as RNI production during the acute phase of infection with T. cruzi parasites. Further, deletion of the functional TLR2 gene had no major impact on parasitemia nor on mortality. In contrast, the MyD88(-/-) mice had a diminished cytokine response and RNI production upon acute infection with T. cruzi. More importantly, we show that MyD88(-/-) mice are more susceptible to infection with T. cruzi as indicated by the higher parasitemia and accelerated mortality, as compared with the wild-type mice. Together, our results indicate that T. cruzi parasites elicit an alternative inflammatory pathway independent of TLR2. This pathway is partially dependent on MyD88 and necessary for mounting optimal inflammatory and RNI responses that control T. cruzi replication during the early stages of infection.

187 citations

Journal ArticleDOI
TL;DR: The Brazilian Longitudinal Study of Adult Health (ELSA-Brasil), a cohort study of 15,105 Brazilian public servants reflects the reality of high prevalences of diabetes, hypertension and the main chronic diseases risk factors.
Abstract: Las enfermedades cronicas no transmisibles representan la mayor carga de morbimortalidad en Brasil. En 2011, el Ministerio de Salud Brasileno lanzo un Plan de Acciones Estrategicas para Enfrentar las enfermedades cronicas no transmisibles, enfatizando acciones poblacionales para controlar las enfermedades cardiovasculares, diabetes, cancer y enfermedad respiratoria cronica, predominantemente por el control del cigarro, inactividad fisica, alimentacion inadecuada y uso perjudicial de alcohol. A pesar de la produccion cientifica significativa sobre tales enfermedades y sus factores de riesgo en Brasil, pocos son los estudios de cohorte en este tema. En este contexto, el Estudio Longitudinal de la Salud del Adulto (ELSA-Brasil) acompana 15.105 servidores publicos del pais. Sus datos reflejan la realidad brasilena de altas prevalencias de diabetes e hipertension y de los factores de riesgo. La diversidad de las informaciones producidas permitira profundizar el entendimiento causal de tales enfermedades y subsidiar politicas publicas para enfrentarlas.

187 citations


Authors

Showing all 42077 results

NameH-indexPapersCitations
Michael Marmot1931147170338
Pulickel M. Ajayan1761223136241
Alan D. Lopez172863259291
Jens Nielsen1491752104005
Mildred S. Dresselhaus136762112525
Jing Kong12655372354
Mauricio Terrones11876061202
Michael Brammer11842446763
Terence G. Langdon117115861603
Caroline A. Sabin10869044233
Michael Brauer10648073664
Michael Bader10373537525
Michael S. Strano9848060141
Pablo Jarillo-Herrero9124539171
Riichiro Saito9150248869
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023111
2022624
20215,709
20205,955
20195,270
20185,020